@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_head {
  this: np:hasAssertion dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_assertion ;
    np:hasProvenance dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_provenance ;
    np:hasPublicationInfo dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_assertion a np:Assertion .
  dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_provenance a np:Provenance .
  dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_assertion {
  miriam-gene:3046 a ncit:C16612 .
  lld:C0002895 a ncit:C7057 .
  dgn-gda:DGN7baae0112cbe1049f3b21056013f26e2 sio:SIO_000628 miriam-gene:3046 , lld:C0002895 ;
    a sio:SIO_001121 .
}
dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_provenance {
  dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_assertion dcterms:description "[We have reviewed the methodology for an accurate quantitation of Hb F in the blood of patients with sickle cell anemia, values observed in hundreds of patients of different (racial or ethnic) backgrounds and with differences in severity of the disease, and the various factors that affect the level of Hb F. The latter include sex, age, genetic background or chromosomal haplotypes, variations in the sequences of the locus control region(s) 5' to the epsilon-globin gene, and the presence of an alpha chain deficiency or alpha-thalassemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:7679078 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP588365.RARTV_qDBTtUaXAb2jqvhVK0nq_PXZZ8kSNgHCqUIyBCg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:54+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}